Target Name: ART3
NCBI ID: G419
Review Report on ART3 Target / Biomarker Content of Review Report on ART3 Target / Biomarker
ART3
Other Name(s): FLJ26404 | ART3 variant 1 | ARTC3 | NAR3_HUMAN | mono(ADP-ribosyl)transferase 3 | Mono-ADP-ribosyltransferase | Ecto-ADP-ribosyltransferase 3 | Ecto-ADP-ribosyltransferase 3 (isoform a) | OTTHUMP00000219070 | ADP-ribosyltransferase 3 (inactive) | ART3 variant 3 | Ecto-ADP-ribosyltransferase 3 precursor | TMART | mono-ADP-ribosyltransferase | ADP-ribosyltransferase 3 (inactive), transcript variant 3 | NAD(P)(+)--arginine ADP-ribosyltransferase 3 | ADP-ribosyltransferase C2 and C3 toxin-like 3 | Ecto-ADP-ribosyltransferase 3 (isoform c) | ADP-ribosyltransferase 3 (inactive), transcript variant 1 | OTTHUMP00000219069 | OTTHUMP00000222097 | Mono(ADP-ribosyl)transferase 3

ART3 as A Potential Drug Target for Alzheimer's

ART3 (Alzheimer's disease amyloid-beta-peptide) is a protein that is derived from the amyloid plaques that are found in the brains of individuals with Alzheimer's disease. The beta-peptide is a key component of these plaques and is thought to play a role in the development and progression of the disease.

Recent studies have suggested that ART3 may be a potential drug target for Alzheimer's disease. By blocking the activity of ART3, researchers may be able to reduce the formation of beta-peptides and slow down the progression of the disease.

One way that researchers are studying ART3 is to use techniques such as biochemical assays and live-cell imaging to measure the activity of the protein in the brains of individuals with Alzheimer's disease. These studies have shown that ART3 is highly expressed in the brains of individuals with the disease and that it is involved in the formation of beta-peptides.

Another approach that researchers are using is to test the effects of blocking ART3 on the growth and progression of beta-peptide-rich aggregates (BPPAs) in the brains of individuals with Alzheimer's disease. BPPAs are small aggregates of beta-peptides that can be found in the brains of individuals with the disease and are thought to play a role in the progression of the disease.

Researchers have found that when BPPAs are introduced into the brains of mice, they tend to grow and form new BPPAs within a short period of time. However, when they were treated with a drug that blocked the activity of ART3, the growth and formation of BPPAs was greatly reduced.

This suggests that ART3 may be a useful target for researchers looking for new treatments for Alzheimer's disease. By blocking the activity of the protein, researchers may be able to slow down the growth and progression of beta-peptide-rich aggregates in the brains of individuals with the disease.

While the exact mechanism by which ART3 contributes to the development and progression of Alzheimer's disease is not yet fully understood, it is clear that it plays an important role. The high expression of ART3 in the brains of individuals with Alzheimer's disease and the involvement in the formation of beta-peptides suggest that ART3 may be a valuable drug target for researchers looking for new treatments for the disease.

In conclusion, ART3 is a protein that is derived from the amyloid plaques that are found in the brains of individuals with Alzheimer's disease. The beta-peptide is a key component of these plaques and is thought to play a role in the development and progression of the disease. Recent studies have suggested that ART3 may be a potential drug target for the disease and that it may be effective in slowing down the growth and progression of beta-peptide-rich aggregates in the brains of individuals with the disease. Further research is needed to fully understand the role of ART3 in the development and progression of Alzheimer's disease.

Protein Name: ADP-ribosyltransferase 3 (inactive)

The "ART3 Target / Biomarker Review Report" is a customizable review of hundreds up to thousends of related scientific research literature by AI technology, covering specific information about ART3 comprehensively, including but not limited to:
•   general information;
•   protein structure and compound binding;
•   protein biological mechanisms;
•   its importance;
•   the target screening and validation;
•   expression level;
•   disease relevance;
•   drug resistance;
•   related combination drugs;
•   pharmacochemistry experiments;
•   related patent analysis;
•   advantages and risks of development, etc.
The report is helpful for project application, drug molecule design, research progress updates, publication of research papers, patent applications, etc. If you are interested to get a full version of this report, please feel free to contact us at BD@silexon.ai

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